FDA 510(k), K002571, MULITPLE MALE LATX CONDOM

510(K) Number: K002571
Device Name: MULITPLE MALE LATX CONDOM
Manufacturer: PLEASURE LATEX PRODUCTS SDN. BHD.
Device Classification Name: condom
Regulation Number: 884.5300
Classification Product Code: HIS
Date Received: 08/18/2000
Decision Date: 11/16/2000
Regulation Medical Specialty: Obstetrics/Gynecology

Total pages: 86
Fully redacted pages: 33
Content pages: 53